FDA UDI In Commercial Distribution 🇺🇸 United States

TELEFLEX

DI: 24026704667172 · Model: IPN055323 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TELEFLEX
Primary DI
24026704667172
Version / Model
IPN055323
Catalog Number
70685
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-31
Public Version
1
Public Version Date
2019-11-08
Public Version Status
New
Public Device Record Key
d0b5d180-c2dd-483e-b882-24b6d94d0dcc

Device Description

Applier, Large - 8 - 55

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GDO Applier, surgical, clip

GMDN Terms

Code Name
35798 Open-surgery ligation clip applier

Identifiers

Type ID
Direct Marking 14026704667175
Primary 24026704667172

Customer Contacts